דלג לתוכן הראשי

CRA II

ICON plcתל אביב-יפו, מחוז תל אביב, ישראללא צויןFull-timeדרגה: דרגת ביניים

פורסם 21 במאי · 0 מועמדים

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תובנת Willbi

התפקיד במילים פשוטות

בתפקיד זה, תהיה אחראי על ניטור ניסויים קליניים, כולל ביקורי אתר, הבטחת עמידה בפרוטוקול ובטיחות המטופל. תעבוד בשיתוף פעולה עם חוקרים וצוותי אתר כדי להבטיח התנהלות חלקה של המחקר, ותבצע סקירת נתונים ופתרון שאילתות.

חובה
  • relevant clinical trial monitoring experience
  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills
יתרון

    חולץ מתיאור המשרה · מתעדכן אוטומטית

    למי זה מתאים

    התפקיד מתאים לבעלי תואר ראשון בתחום מדעי או רפואי, עם ניסיון של שנתיים לפחות כעמית מחקר קליני. נדרש ידע מעמיק בתהליכי ניסויים קליניים וכישורי ארגון ותקשורת חזקים.

    תיאור המשרה המלא

    המשרה המקורית · נשמר לעיון

    Clinical Research Associate, Israel

    ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

    As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

    What You Will Do

    You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

    Key Responsibilities Include

    Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

    Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

    Collaborating with investigators and site staff to facilitate smooth study conduct.

    Performing data review and resolution of queries to maintain high-quality clinical data.

    Contributing to the preparation and review of study documentation, including protocols and clinical study reports

    Your Profile

    You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

    Required Qualifications And Experience

    Bachelor's degree in a scientific or healthcare-related field.

    Minimum of 2 years of experience as a Clinical Research Associate.

    In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

    Strong organizational and communication skills, with attention to detail.

    Ability to work independently and collaboratively in a fast-paced environment.

    Willingness to travel as required (approximately 60%)

    What ICON Can Offer You

    Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

    In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

    Our Benefits Examples Include

    Various annual leave entitlements

    A range of health insurance offerings to suit you and your family’s needs.

    Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

    Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

    Life assurance

    Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

    Visit our careers site to read more about the benefits ICON offers.

    At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

    If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

    Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

    Are you a current ICON Employee? Please click here to apply

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    אודות ICON plc
    פרופיל החברה · בקרוב

    ביקורות עובדים · בקרובעוד משרות ב-ICON plc

    שאלות על המשרה

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